A biochemically-realisable relational model of the self-manufacturing cell. (September 2021)

• Record Type: Journal Article
• Authors: Hofmeyr, Jan-Hendrik S.
• Is Part Of: Bio systems. Volume 207(2021)
• Publication Date: 2021-09
• Subjects: Relational biology -- Self-manufacture -- Fabrication -- Self-assembly -- Metabolism-repair systems -- Closure to efficient causation -- Autopoiesis -- Formal cause; Biological systems -- Periodicals; Biology -- Periodicals; Biology -- Periodicals; Evolution -- Periodicals; Biologie -- Périodiques; Évolution -- Périodiques; 570
• DOI: 10.1016/j.biosystems.2021.104463
• Languages: English
• ISSNs: 0303-2647

Abstract

Abstract: As shown by Hofmeyr, the processes in the living cell can be divided into three classes of efficient causes that produce each other, so making the cell closed to efficient causation, the hallmark of an organism. They are the enzyme catalysts of covalent metabolic chemistry, the intracellular milieu that drives the supramolecular processes of chaperone-assisted folding and self-assembly of polypeptides and nucleic acids into functional catalysts and transporters, and the membrane transporters that maintain the intracellular milieu, in particular its electrolyte composition. Each class of efficient cause can be modelled as a relational diagram in the form of a mapping in graph-theoretic form, and a minimal model of a self-manufacturing system that is closed to efficient causation can be constructed from these three mappings using the formalism of relational biology. This fabrication-assembly or ( F, A )-system serves as an alternative to Robert Rosen's replicative metabolism-repair or ( M, R )-system, which has been notoriously problematic to realise in terms of real biochemical processes. A key feature of the model is the explicit incorporation of formal cause, which arrests the infinite regress that plagues all relational models of the cell. The ( F, A )-system is extended into a detailed relational model of the self-manufacturing cell that has a clear biochemical realisation. This ( F, A ) cell model allows the interpretation and visualisation of concepts such as the metabolism and repair components of Rosen's ( M, R )-system, John von Neumann's universal constructor, Howard Pattee's symbol-function split via the symbol-folding transformation, Marcello Barbieri's genotype–ribotype–phenotype ontology, and Tibor Gánti's chemoton.